Variant (rsID / SNP)

rs62635037

rs62635037 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR143. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

GPR143Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Cytoband: Xp22.2
HGVS: NM_000273.3(GPR143):c.686G>T (p.Gly229Val)
Allele change: Missense_G229V

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.